Manufacture of manganese carbonyl



United States Patent MANUFACTURE OF MANGANESE CARBONYL Harold E. Podall, Baton Rouge, La., assignor to Ethyl Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Dec. 29, 1958, Ser. No. 783,201

. '6 Claims. (Cl. 23-203) This invention relates to metal carbonyls and particularly the manufacture of the manganese pentacarbonyl dimer.

Some procedures for the preparation of certain metal carbonyls have been described in the literature. With particular metals, successful results are obtained by reacting the metal with carbon monoxide at high temperatures and pressures or in certain instances reacting particular metal salts with hydrogen and then carbon monoxide. These procedures are applicable only in limited instances as, for example, with the metals nickel and iron. They likewise leave much to be desired since stringent process techniques are required and the metal or metal compound must be in particular form.

The procedures likewise are not available to the more difiicultly produced metal carbonyls. The most satisfactory procedure devised as yet for the preparation of manganese pentacarbonyl dimer involves the reaction of manganese salts with a Grignard reagent and then reacting the product so-produced with carbon monoxide. This two-step procedure has been improved by judicious choice of the Grignard reagent employed. However, even with these improvements the process sufiers particular disadvantages which are to be overcome. For example, for some unexplained reason the process is relatively independent of variables such as pressure beyond a certain point. In other words, essentially no change is obtained in the rate of reaction or the yield when these variables are changed. Another inherent disadvantage in the process is that the yields are such that commercial employment of the procedure is not practical. A stifi further disadvantage of this process is that, during the course of reaction, by-product metallic manganese is obtained and this material cannot be converted to the desired carbonyl compound.

Accordingly, it is an object of this invention to provide a new and novel process for the preparation of manganese pentacarbonyl dimer. A particular object is to provide a procedure whereby manganese pentacarbonyl dimer is obtained in higher yield than heretofore available. Other objects and advantages will be apparent from the following description and appended claims.

The above and other objects of this invention are achieved by reacting a salt of manganese, including oxides or sulfides, carbon monoxide, and a reducing metal of groups I-A, II and III-A, in the presence of catalytic quantities of an organometallic compound of said reducing metals. Best results are obtained using from about 0.1-30 mole percent of the organometallic compound, based on the moles of reducing metal employed. Furtherparticular advantage is achieved when the organometallic compound is a compound of aluminum. Thus, one embodiment comprises the reaction of a salt, especially halides and salts of organic acids or manganese with a group I-A, II or III-A metal in the presence of an organoaluminum compound, particularly alkyl aluminum compounds, and carbon monoxide.

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When employing the procedure of this invention, simultaneous reaction of the metal salt, the .reducing metal, the organometallic compound and the carbon monoxide is obtained, thus providing an enhancement in yield, faster'reaction rates and minimization of undesirable byproduct manganese metal. The stringent processing operations of the prior art techniques are not required and the difiiculty of producing by-product metal is overcome. Of particular importance, the use of catalytic quantities of the organometallic compounds reduces appreciably the quantity of reducing metal required and, at the same time, increases, usually from 2 to 10 times, the conversion of manganese salt to the desired manganese pentacarbonyl dimer.

The salts of manganese employable are many and varied, including both inorganic and organic salts. For the purposes herein, the oxides and sulfides of these metals are also intended in the terminology salts, although such are not truly salts. Typical examples of the inorganic salts are the halides, phosphates, sulfites, sulfates, nitrates, fluosilicates, carbonates, oxides, sulfides, and the like. The organic salts of manganese include, for example, the carboxylates, e.g. alkyl, aryl, cycloalkyl, and the like carboxylates, the alcoholates, e.g. phenates, alkoxides, and enolates and the thioalcoholates or mercap tides. Among the inorganic salts employable in the process of this invention are manganese bromide, iodide, fluoride and chloride, carbonate, the various oxides, phosphate, fluosilicate, sulfate, sulfide, sulfite, and the like. Among the organic salts of manganese employable are included for example, manganese acetate, benzoate, citrate, formate, lactate, oxalate, malonate, valerate, naphthenate, oleate, acetylacetonate, toluate, phenate, ethylate, decanoate, thiomethylate, and the like. It is to be understood that all valence states of manganese are intended. In general, inthe organic type salts, the organo portion will contain between 1 to 25 carbon atoms in each radical although higher molecular weight acid salts can be employed.

For best results the halide salts and organic acid salts of manganese are especially preferred. In those instances wherein the metal salt is a solid in the reaction mixture, it is generally desirable to employ such materials in finely divided form of the order of about 1,000 microns or less.

The reducing metal employed in the process of this invention can be any of the metals, or mixtures thereof, of groups I-A, II and III-A of the periodic chart of the elements (Handbook of Chemistry and Physics, 36th edition, pages 392-393, Chem. Rubber Publishing Go). For economic reasons, the preferred reducing metals are sodium, magnesium, aluminum and zinc. Other suitable metals are lithium, potassium, beryllium, calcium, boron,

gallium, cadmium, mercury and the other metals of' these groups. These metals are usually employed in finely divided form, and frequently, particularly with metals such as sodium, are used in a dispersion in an inert diluent.

The organometallic catalyst employed is one of an element of groups IA, II and III-A of the periodic table. Such elements include boron, aluminum, gallium, indium and thallium, discussed immediately above. The organometallic compound will usually contain alkyl and/ or aryl groups having between about 1 to 25 carbon atoms in each organic radical. In general, the metal is attached to atleast one carbon atom of an organic radical. The polyvalent metals can additionally be attached to other elements, as for example, the halides, hydrogen or another metal, particularly the group I-A metals. Typical examples of such organometallic compounds include the following: methyl sodium, ethyl sodium, phenyl sodium, naphthyl sodium, ethyl lithium, phenyl lithium, tolyl lithium, ethyl potassium, ethyl rubidium, methylcesium, diethyl beryllium, dimethyl magnesium, diethyl magnesium, diphenyl magnesium, ethyl magnesium chloride, ethyl magnesium hydride, dioctyl magnesium, diethyl calcium, diethyl strontium, diethyl barium, trirnethylboron, triethylboron, ethylboron difluoride, sodium tetraethylborate, trimethylaluminum, triethylaluminum, methyldiethylaluminum, tripropylaluminum, dimethylhexylaluminum, methylethyloctylaluminum, triisooctylaluminum, diethylaluminum hydride, methylaluminum dihydride, triisobutylaluminum, diisobutylaluminum hydride, octylaluminum dihydride, sodium aluminum tetraethyl, lithium aluminum tetraethyl, potassium aluminum triethyl hydride, sodium aluminum tetrabutyl, potassium aluminum dioctyl dihydride, dimethylaluminum chloride, ethyl aluminum dichloride, ethyl aluminum sesquichloride, trimethylgallium, triethylgallium, methyldiethylgallium, tripropylgallium, trioctylgallium, triisobutylgallium, trimethylindium, triethylindium, tripropylindium, triisobutylindium, triphenylaluminum, sodium aluminum diethyl acetylide, cyclohexyldiethylaluminurn, tribenzyl aluminum, triethyl thallium, triphenylthallium, and the like.

For practical purposes and best results, the alkylaluminum compounds are preferably employed. These compounds are more stable, more readily available and are of higher selectivity. Preferably, each alkyl group therein will contain from 1 up to and including about 8 carbon atoms.

In general, the process is readily performed by placing the manganese salt, the reducing metal, the organometallic compound and the carbon monoxide into a reaction vessel in a suitable inert atmosphere and, if desired, in the presence of an essentially inert liquid medium. The carbon monoxide is generally pressurized into the reactor. The reaction mixture is likewise usually agitated to provide adequate contact. In most instances, the simultaneous reaction of these materials will take place at room temperature although heating is preferred to efiect greater reaction rates. At the completion of the reaction, the product is recovered in a conventional manner such as distillation, sublimation, or separation of by-products leaving the product in the liquid medium, when employed, which can then be recovered by concentration and filtration. Alternatively, it is frequently desired to feed the reducing metal to the reaction mixture periodically or continuously during the reaction period.

The process of this invention will be more fully understood by reference to the following examples. In all examples, parts and yields are by weight.

Example I To a reactor equipped with external heating means, internal agitation, means for maintaining pressure, and

means for admitting and discharging reactants and products, is added 0.05 mole of manganous chloride, 0.25 atom of powdered aluminum, and 0.0025 mole of triethylaluminum in a large excess of tetrahydrofuran under an inert atmosphere of nitrogen. The reactor is then pressurized with 2500 p.s.i.g. of carbon monoxide and heated with continuous agitation to 120 C. These conditions are maintained for a period of four hours. At the end of this period, after cooling to room temperature, the gases in the reactor are vented to the atmosphere and the mixture is quenched with water and dilute hydrochloric acid. The mixture is then extracted with diethyl ether, and the ether layer is then separated and dried. This dry layer is then subjected to distillation to concentrate the product. In this manner manganese pentacarbonyl dimer is obtained in high yield.

Similar results are obtained when the above example is repeated while employing a carbon monoxide pressure of 500 p.s.i.g. with a reaction period of ten hours;

4 Example I1 conducted in diethyl ether solvent at a temperature of 25 C. After 20 hours, the manganese pentacarbonyl v C. for hours.

is recovered by steam distillation. A good yield of manganese pentacarbonyl is obtained.

Example 111 Manganous chloride (0.05 mole) is reacted with carbon monoxide in the presence of metallic aluminum (0.15 atom) and catalytic quantities of triethylaluminum (0.0025 mole). The carbon monoxide (3000 p.s.i.g.) is added to the reactor and the reaction heated to Diethyl ether is again employed as the solvent. The manganese pentacarbonyl dimer is recovered by steam distillation.

Example IV Manganous acetate (0.01 mole) and powdered aluminum metal (0.033 atom) is added to a reactor along with an excess of diethyl ether. To this mixture is added 0.002 mole of triethylaluminum. The reactor is closed and pressurized with 3000 p.s.i.g. carbon monoxide pressure, and heated to a temperature of 80 C. for 20 hours. Excellent conversions of the manganous acetate to manganese pentacarbonyl dimer are obtained.

Example V Manganese acetate (0.05 mole) is reacted with carbon monoxide (5000 p.s.i.g.) in the presence of powdered magnesium (0.10 atom) which is wetted with 0.02 mole of triisobutyl aluminum and an excess of isopropyl ether. The reaction is conducted at a temperature of C. for six hours giving an excellent yield of manganese pentacarbonyl dimer.

Example VII Manganous chloride (0.10 mole) is reacted with carbon monoxide (1000 p.s.i.g.) in m-xylene while continuously feeding a sodium dispersion in the m-xylene containing catalytic quantifies of phenyl sodium over a period of two hours. The total quantity of sodium fed to the reaction is 0.20 atom, which contains 0.005 mole of the phenyl sodium. The mangagese pentacarbonyl dimer is recovered by steam distillation in good yields.

Example VIII Manganous fluoride (0.03 mole), zinc dust (0.18 atom equivalents), diethyl zinc (0.003 mole) and an excess of n-heptane are charged to the reactor and the reactor thereafter pressurized with 3000 p.s.i.g. carbon monoxide pressure. The reaction mixture is heated for 20 hours at 150 C. while continuously stirring the reaction mixture. The manganese pentacarbonyl dimer is steam distilled from the reaction mixture and recovered in excellent yield.

Example IX Manganese sulfide (0.02 mole) is reacted in diethylene glycol dimethyl ether solvent with 0.6 atom of aluminum, 0.002 mole of diethyl aluminum chloride and 5000 p.s.i.g. of carbon monoxide pressure. The reaction conducted at a temperatureof 180 C. for 20 hours giving'an excellent yield of the desired manganese pentacarbonyl dimer.

Example X Manganous bromide (0.2 mole) is reacted with carbon monoxide at a pressure of 5000 p.s.i.g. The reaction mixture contains 0.60 atom of lithium and 0.06 mole of Example XI Example I is repeated except that the reaction is conducted in diethylene glycol dimethyl ether solvent at a temperature of 180 C. Similar results are obtained.

Example XII Manganous methoxide is reacted in anisole solvent with carbon monoxide (3000 p.s.i.g.) in the presence of Zinc dust and triethyl aluminum. The zinc dust is employed in a concentration of 5 atoms per mole of manganese salt. The reaction is conducted at 160 C. and gives an excellent yield of manganese pentacarbo-nyl in about 20 hours.

For the organometallic compounds employed in the above examples one can substitute dimethylaluminum hydride, tribenzylaluminum, tricyclohexylindium, ethylaluminum sesquichloride, diethylaluminum bromide, triethyl gallium, triphenyl gallium, boron, or indium, tri methylindium and the like and obtain similar results.

The temperature at which the reaction is conducted is not critical and generally temperatures between to about 200 C. are employed. In general, the higher the temperature the faster the reaction rate. Accordingly, for such purposes it is preferred to operate at temperatures ranging from 75 to 175 C., depending upon the reactants employed. Likewise, the pressure can be varied over a wide range from superatmosphen'c to subatmospheric pressures. Ordinarily, since the carbon monoxide is a gas, pressures above atmospheric are employed. A preferred range is between 500 to 4000 p.s.i. in order to obtain optimum results.

The time of reaction will likewise depend somewhat upon the other conditions under which the reaction is conducted although times between about 1 minute to 20 hours are generally quite adequate. In order to minimize side effects, it is preferred to conduct the reaction for a period of from 5 minutes to 6 hours.

The proportions of the reactants can likewise be varied and generally are based upon the metal salt. In this connection between about 1 gram atom to 6 gram atoms and higher of the reducing metal are employed per gram mole of the metal salt. However, as the temperature is increased the number of gram atoms of metal generally can be decreased. Where excesses of the metal are employed, such excesses may be recovered and reused. The organometallic compound is employed in catalytic quantities, i.e., usually from about l-15 mole percent of the reducing metal. Lower and higher concentrations can be used. However, at lower concentrations, the beneficial results of the catalysts are diminished whereas, at higher concentration, no proportionate improvement is obtained. The carbon monoxide is generally employed in stoichiometric amounts, although excesses can be beneficially employed.

While the above examples indicate that an organic diluout is employed, it is to be understood that such are not essential. In general, when such are employed they should be essentially inert to the reactants. Furthermore, it is desirable, but not necessary, that they exhibit solubility for one or all of the reactants. Among such organic diluents which can be employed are included the hydrocarbons, ethers and amines. Among the hydrocarbons included are, for example, nonanes, octadecanes, hexanes, toluene, benzene, xylene, mesitylene and mixed hydrocarbons such as gasoline, diesel oil and the like petroleum fractions. Among the others employable are included, for example, the non-aromatics, aromatics and polyethers including, for example, di-sec-butyl ether, di-n-heptyl ether, di-isopropyl ether, ethylisoamyl ether, methylphenyl ether (anisole), p-tolyl ether, ethylphenyl ether, tetraethylene glycol dimethyl ether, and the dimethyl, diethyl, and di-nbutyl ethers of diethylene glycol. Among the amines which are employable are included dimethyl amine, di-

ethyl amine, dioctyl amine, diphenyl amine, dicyclohexyl amine, methylethyl amine, p-methyl pyridine, o-methyl pyridine, 2,6-dimethylpyridine, isoquinoline, trimethyl amine, triethyl amine, tributyl amine, tricyclohexyl amine and the like.

The coordinating solvents, especially the ethers, are particularly preferred since these materials exhibit a reaction promoting effect.

The process provides products which are of considerable use. These products can be, for example, subjected to high temperatures, thereby providing decomposition to obtain manganese in finely divided form. Another particular use for the compounds produced according to the process of this invention is as additives to fuels, especially for internal combustion engines and the like. For example, when suflicient manganese pentacarbonyl is added to commercial gasoline to obtain compositions containing 1 gram of manganese per gallon, the octane number of the gasoline is greatly increased. The products are also useful as chemical intermediates in preparing organometallic compounds. These and other uses will be evident to those skilled in the art.

Having thus described the process of this invention, it is not intended that it be limited except as set forth in the following claims.

I claim:

1. The process for the manufacture of manganese pentacarbonyl dimer which comprises reacting a salt of manganese, carbon monoxide and a reducing metal selected from the group consisting of metals of groups I-A, II and III-A of the periodic chart of the elements in contact with catalytic quantities of an organometallic compound of said reducing metals having organo groups selected from the group consisting of alkyl and aryl groups at a temperature of 0200 C. and at a carbon monoxide pressure above atmospheric and up to about 5,000 p.s.i.g., said organometallic compound having a metal atom bonded directly to a carbon of said organo groups.

2. The process of claim 1 wherein the organometallic compound is an organoaluminum compound.

3. The process of claim 2 wherein the reducing metal is aluminum.

4. The process of claim 1 wherein the reducing metal is sodium.

5. The process of claim 1 wherein the organo group of the organometallic compound is an alkyl group containing from 1 to 8 carbon atoms.

6. The process of claim 1 wherein the metal is in finely divided form, the organometallic compound is present in a concentration of from 1 to 15 mole percent of said metal and the reaction is carried out in an inert liquid medium.

References Cited in the file of this patent UNITED STATES PATENTS 2,739,169 Hagemeyer Mar. 20, 1956 2,822,247 Hnizda Feb. 4, 1958 2,825,631 Lynch Mar. 4, 1958 

1. THE PROCESS FOR THE MANUFACTURE OF MANGANESE PENTACARBONYL DIMER WHICH COMPRISES REACTING A SALT OF MANGANESE, CARBON MONOXIDE AND A REDUCING METAL SELECTED FROM THE GROUP CONSISTING OF METALS OF GROUPS I-A, II AND III-A OF THE PERIODIC CHART OF THE ELEMENTS IN CONTACT WITH CATALYTIC QUANTITIES OF AN ORGANOMETALLIC COMPOUND OF SAID REDUCING METALS HAVING ORGANO GROUPS SELECTED FROM THE GROUP CONSISTING OF ALKYL AND ARYL GROUPS AT A TEMPERATURE OF 0-200*C. AND AT A CARBON MONOXIDE PRESSURE ABOVE ATMOSPHERIC AND UP TO ABOUT 5,000 P.S.I.G., SAID ORGANOMETALLIC COMPOUND HAVING A METAL ATOM BONDED DIRECTLY TO A CARBON OF SAID ORGANO GROUPS. 